Borse Mrudula S, Dong Olivia M, Polasek Melissa J, Farley Joel F, Stouffer George A, Lee Craig R
Division of Pharmaceutical Outcomes & Policy, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Division of Pharmacotherapy & Experimental Therapeutics, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Pharmacogenomics. 2017 Aug;18(12):1155-1166. doi: 10.2217/pgs-2017-0075. Epub 2017 Jul 26.
Determine whether using CYP2C19 genotype to optimize antiplatelet therapy selection is cost effective over the initial 30 days and 1-year following percutaneous coronary intervention.
MATERIALS & METHODS: A cost-effectiveness analysis compared 30-day and 1-year outcomes and cost across three treatment strategies (universal clopidogrel, universal prasugrel, genotype-guided) in a hypothetical cohort.
Base-case scenario results at 30 days indicated that the incremental cost per major cardiovascular or bleeding event avoided for genotype-guided treatment was US$8525 and US$42,198 compared with universal clopidogrel and prasugrel, respectively. Probabilistic sensitivity analysis demonstrated that genotype-guided treatment was cost effective over 30 days and 1 year in 62 and 70% of simulations, respectively.
Implementing a CYP2C19 genotype-guided approach to antiplatelet therapy could have a positive economic impact by preventing readmissions following percutaneous coronary intervention.
确定在经皮冠状动脉介入治疗后的最初30天及1年内,使用CYP2C19基因分型来优化抗血小板治疗方案的选择是否具有成本效益。
一项成本效益分析比较了假设队列中三种治疗策略(通用氯吡格雷、通用普拉格雷、基因分型指导)在30天和1年时的结局及成本。
30天的基础病例分析结果表明,与通用氯吡格雷和普拉格雷相比,基因分型指导治疗避免每例主要心血管或出血事件的增量成本分别为8525美元和42,198美元。概率敏感性分析表明,在分别62%和70%的模拟中,基因分型指导治疗在30天和1年内具有成本效益。
实施CYP2C19基因分型指导的抗血小板治疗方法,可能通过预防经皮冠状动脉介入治疗后的再入院而产生积极的经济影响。